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A method for predicting the risk of developing pre-eclampsia and its severity on genetic data

机译:根据遗传数据预测先兆子痫的风险及其严重性的方法

摘要

Risk prediction method of pre-eclampsia and its degree of severity in females Russian nationality, natives Central Chernozemya comprising blood sampling, characterized in that the DNA is isolated from peripheral venous blood by analyzing the genetic polymorphisms + 46G / A ADRB2, 4a / 4b eNOS, G460W ADD1 K198N and ET-1 and predict increased risk of developing pre-eclampsia in the presence of the allele 198K ET-1; increased risk of developing preeclampsia, moderate and severe levels of severity in the presence of a combination of genetic variants with 4a4a eNOS 198N ET-1; increased risk of developing preeclampsia, moderate and severe degrees of severity in the presence of a genotype 460WW ADD1; lower risk of preeclampsia in the presence of combinations of genetic variants + 46A ADRB2, 198N ET-1, 4b eNOS; 4b eNOS, 198N ET-1, + 46A ADRB2, 460G ADD; 198N ET-1, + 46A ADRB2, 460G ADD1; 4b eNOS, 460G ADD1, 198N ET-1; + 46A ADRB2, 198N ET-1; 198N ET-1, 4b eNOS; low risk of developing pre-eclampsia moderate and severe levels of severity in the presence of a combination of genetic variants 4b eNOS, 460G ADD1.
机译:俄裔女性先兆子痫的风险预测方法及其严重程度,包括采血的中部切尔诺兹米亚人,其特征是通过分析遗传多态性+ 46G / A ADRB2、4a / 4b eNOS从外周静脉血中分离DNA ,G460W ADD1 K198N和ET-1预测存在等位基因198K ET-1时发生先兆子痫的风险增加;在遗传变异体与4a4a eNOS 198N ET-1结合存在的情况下,发生先兆子痫,中度和重度严重程度的风险增加;在存在基因型460WW ADD1的情况下发生先兆子痫,中度和重度严重程度的风险增加;在存在遗传变异+ 46A ADRB2、198N ET-1、4b eNOS组合的情况下,先兆子痫的风险降低; 4b eNOS,198N ET-1,+ 46A ADRB2、460G添加; 198N ET-1,+ 46A ADRB2,460G ADD1; 4b eNOS,460G ADD1、198N ET-1; + 46A ADRB2,198N ET-1; 198N ET-1,4b eNOS;在存在遗传变异体4b eNOS,460G ADD1组合的情况下,发生先兆子痫的风险低至中等和严重水平。

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